Polysilanes chemical properties

The chemistry of compounds containing Si-Si bond(s) is an intriguing subject in the field of organosilicon chemistry because Si-Si bonds have unique physical and chemical properties. The reactivities of Si-Si bonds is often compared with those of carbon-carbon double bonds. The current interest in polysilanes in material science stems from the fact that they exhibit unusual properties implying considerable electron delocalization in the polymer chain [62]. This section concerns with the unique elecrochemical properties of compounds containing Si-Si bonds (Sect. 2.4). 

The most intriguing difference between the chemical properties of cyclopolysilanes and those of cycloalkanes is the ability of the former to form either anion or cation radicals upon one-electron reduction or oxidation, respectively. For example, the cyclic pentamer (Mc2Si)5 is reduced to the corresponding radical anion by sodium-potassium alloy in diethyl ether [see eqn (4.1) in Section 4.1.3], whereas the hexamer (Me2Si)6 is oxidised by aluminium trichloride in dichlor-omethane to the corresponding cation radical. In both cases the EPR spectra of the radical ions can be interpreted in terms of a-electron delocalisation over the entire polysilane ring (see Section 10.1.4.1). In this respect, the cyclosilanes resemble aromatic hydrocarbons rather than their aliphatic analogues. 

The condensation of secondary silanes requires more rigorous conditions and no catalyst has yet been reported to couple tertiary silanes efficiently [140]. The great interest in polysilane polymers and their potential application come from their unusual electronic, optical, and chemical properties [142], particularly as preceramic materials [143]. The reaction constitutes the only alternative to Wurtz coupling for the formation of silicon-silicon bonds. 

Another important class of photonic materials is polysilanes (Fig. 49.15) [217-222]. In polysilanes the delocalization of (T orbitals of the Si atom along the polymer backbone plays a significant role in their NLO properties. Their physical and chemical properties can be tailored by the choice of an appropriate substituent, which also determines the conformation of the polymer and its solubility. What is of more interest is their transparency in their NLO properties, values of a series of polysilanes are given in Table 49.9. Tables 49.10-49.13 contain y and values of some other third-order materials, namely metallophthalocyanine, bis-metallophthalocyanine, metallonaphthalocyanines, fuller-enes, and j8-carotenes. Although these molecules are not considered as polymers, they are macromolecules that have drawn a considerable amount of attention as third-order NLO materials. For example, the highly stable icosa-... 

ABSTRACT. Polysilanes, (-SiRR -)n, represent a class of inorganic polymers that have unusual chemical properties and a number of potential applications. Currently the most practical synthesis is the Wurtz-type coupling of a dihalosilane with an alkali metal, which suffers from a number of limitations that discourage commercial development. A coordination polymerization route to polysilanes based on a transition metal catalyst offers a number of potential advantages. Both late and early metal dehydrogenative coupling catalysts have been reported, but the best to date appear to be based on titanocene and zirconocene derivatives. Our studies with transition metal silicon complexes have uncovered a number of observations that are relevant to this reaction chemistry, and hopefully important with respect to development of better catalysts. We have determined that many early transition metal silyl complexes are active catalysts for polysilane synthesis from monosilanes. A number of structure-reactivity correlations have been established, and reactivity studies have implicated a new metal-mediated polymerization mechanism. This mechanism, based on step growth of the polymer, has been tested in a number of ways. All proposed intermediates have now been observed in model reactions. 

Figure 9 Thermochromic UV properties of (a) end-graft polysilane 79, (b) dilute solution, and (c) film analogs 80.65 Reprinted with permission from Ebata, K. Furukawa, K. Matsumoto, N. Fujiki, M. Polym. Prepr. (Am. Chem. Soc. Div. Polym. Chem.) 1999, 40, 157-158, 1999 American Chemical Society.

In this section, for convenience, we first deal with the synthesis and some physical properties of permethylated polysilanes, and then synthesis of other peralkylated and partially phenylated methyl polysilanes. Finally, chemical reactions of all such types of compounds will be discussed together. 

The proton NMR spectral data of organopolysilanes have often been published incidental to preparative studies (51, 54, 62, 74, 108, 119, 177, 187, 190). Only recently has a systematic investigation to determine the chemical shifts and coupling constants in linear and cyclic permethylated polysilanes, and to study the effects of substituents on the NMR properties of methyl derivatives of disilane and trisilane been reported (see Table V-VII) (206). 

The preparation of these higher molecular weight polystannanes, and the demonstration that they possess a chemical and mechanical integrity similar to that of the polysilanes (they are, however, much more photosensitive than polysilanes), will no doubt stimulate the further study of their properties and methods for their synthesis. 

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